Canonical Allele Identifier: CA1820609143
Gene: HHLA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132091083T= , CM000670.2:g.132091083T= GRCh38
NC_000008.10:g.133103330T= , CM000670.1:g.133103330T= GRCh37
NC_000008.9:g.133172512T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1484A= MANE Select ENSP00000388322.1:n.449-1484A=
ENST00000673615.1:c.557-1484A= ENSP00000500443.1:n.557-1484A=
ENST00000414222.1:c.449-1484A= ENSP00000388322.1:n.449-1484A=
ENST00000434736.6:c.557-1484A= ENSP00000407107.2:n.557-1484A=
NM_001145095.1:c.449-1484A= NP_001138567.1:n.449-1484A=
NM_001145095.3:c.449-1484A= MANE Select NP_001138567.1:n.449-1484A=